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Identification of encapsulated and non-encapsulated Yersinia pestis by immunofluorescence tests using polyclonal and monoclonal antibodies

Published online by Cambridge University Press:  15 May 2009

A. P. Phillips ,
B. C. Morris ,
D. Hall ,
M. Glenister  and
J. E. Williams
A. P. Phillips
Affiliation:
Chemical Defence Establishment, Porton Down, Salisbury, Wiltshire, SP4 OJQ, UK
B. C. Morris
Affiliation:
Chemical Defence Establishment, Porton Down, Salisbury, Wiltshire, SP4 OJQ, UK
D. Hall
Affiliation:
Chemical Defence Establishment, Porton Down, Salisbury, Wiltshire, SP4 OJQ, UK
M. Glenister
Affiliation:
Chemical Defence Establishment, Porton Down, Salisbury, Wiltshire, SP4 OJQ, UK
J. E. Williams
Affiliation:
Department of Hazardous Microorganisms, Walter Reed Army Institute of Research, Washington DC 20307–5100, USA
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Rabbit polyclonal hyperimmune antibodies to Yersinia pestis, and a mouse monoclonal antibody against the capsular antigen fraction 1 (F1) were compared in immunofluorescence (IF) tests. Fluorescent antibody conjugates were prepared from polyclonal antisera to four F1 positive Y. pestis strains; the conjugated antibody to strain A1122 gave the strongest IF staining of F1 positive and F1 negative Y. pestis strains. Indirect assays were rejected in favour of direct assays utilizing polyclonal and monoclonal reagents because the increased background staining reduced the effective contrast of bacterial visualisation. Polyclonal conjugates gave fairly homogeneous staining of Y. pestis bacterial populations, but in monoclonal assays a skew distribution of fluorescence intensity was observed, the majority of bacteria being poorly stained. The proportion of cells stained well by the monoclonal sufficed for easy identification of Y. pestis of the F1 positive phenotype however, and staining was not affected by washing the bacteria or treating them with formaldehyde. Y. pestis strains of the F1 positive genotype reacted with the monoclonal if bacteria were grown at 37 °C but not if the growth temperature was reduced to 25°C thus preventing capsule production. The polyclonal conjugate reacted with bacteria of these strains that had been grown at either temperature. Strains of F1 negative genotype grown at either temperature. Strains of F1 negative genotype grown at either temperature reacted with the polyclonal conjugate but not with the monoclonal. Cross reactions between the polyclonal reagents and Y. enterocolitica biovar 2, serovar O 8 could not be removed by selective absorption; however, the monoclonal antibody gave no cross reaction.

The F1 phenotypic status of bacterial preparations was verified by ELISA measurement of the fraction 1 antigen concentration. Antigen levels for F1 positive and F1 negative phenotypes differed by about three logs for suspensions of Y. pestis harvested from solid media.

The polyclonal and monoclonal direct IF tests applied to spleen and blood smears of laboratory mice infected with Y. pestis were able to differentiate between lethal infection with an F1 positive strain carrying all four classical virulence determinants, an F1 positive vaccine strain, and an F1 negative strain.

Type
Special Article
Information
Epidemiology & Infection , Volume 101 , Issue 1 , August 1988 , pp. 59 - 73
Copyright
Copyright © Cambridge University Press 1988

References

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